510(k) K083118 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICE
| Applicant | Spinal USA, Pear MS, US |
| Decision | Substantially Equivalent, May 27, 2009 |
| Received | Oct 22, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083118
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.